Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: TMEM246-AS1 (Hsa)
(GRCh38)9:101476407C>T
(Homo sapiens)Allele/Variant
Source: rs201690177
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476407C>T
(GRCh38)9:101476959C>T
(Homo sapiens)Allele/Variant
Source: rs140612519
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476959C>T
(GRCh38)9:101477055C>T
(Homo sapiens)Allele/Variant
Source: rs372713797
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101477055C>T
(GRCh38)9:101477080T>C
(Homo sapiens)Allele/Variant
Source: rs182375791
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101477080T>C
(GRCh38)9:101476746T>C
(Homo sapiens)Allele/Variant
Source: rs763973060
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476746T>C
(GRCh38)9:101477056G>C
(Homo sapiens)Allele/Variant
Source: rs575803870
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101477056G>C
(GRCh38)9:101475910G>A
(Homo sapiens)Allele/Variant
Source: rs769427864
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101475910G>A
(GRCh38)9:101476311C>T
(Homo sapiens)Allele/Variant
Source: rs1407947533
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476311C>T
(GRCh38)9:101475940C>A
(Homo sapiens)Allele/Variant
Source: rs775557693
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101475940C>A
(GRCh38)9:101476033C>G
(Homo sapiens)Allele/Variant
Source: rs140582774
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476033C>G
(GRCh38)9:101476723G>T
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.101476723G>T
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476723G>T
(GRCh38)9:101476065G>A
(Homo sapiens)Allele/Variant
Source: rs746600970
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476065G>A
(GRCh38)9:101476932C>T
(Homo sapiens)Allele/Variant
Source: rs751875311
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476932C>T
(GRCh38)9:101476794G>A
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.101476794G>A
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476794G>A
(GRCh38)9:101476627T>G
(Homo sapiens)Allele/Variant
Source: rs1291116519
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476627T>G
(GRCh38)9:101476774T>C
(Homo sapiens)Allele/Variant
Source: rs139396550
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476774T>C
(GRCh38)9:101476573C>A
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.101476573C>A
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476573C>A
(GRCh38)9:101476144G>A
(Homo sapiens)Allele/Variant
Source: rs766828805
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476144G>A